Product code KIZ— Hematology

FDA has cleared 8 devices under product code KIZ between 1979 and 1989, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19891 clearance
• 19872 clearances
• 19852 clearances
• 19821 clearance
• 19792 clearances

• Nunc, Inc.1 clearance
• Lifetrac, Inc.1 clearance
• Isratech Marketing Corp.1 clearance
• Howmedica Corp.1 clearance
• Dynatech Laboratories, Inc.1 clearance
• Dynatech Corp.1 clearance
• Corning Medical & Scientific1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance

• K890542 — MULTIWELL CULTURE PLATE INSERTSBd Becton Dickinson Vacutainer Systems Preanalytic·1989-02-14
• K873891 — TISSUE CULTURE DISHESNunc, Inc.·1987-11-25
• K871483 — TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHESIsratech Marketing Corp.·1987-04-29
• K854724 — CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATELifetrac, Inc.·1985-12-13
• K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATESCorning Medical & Scientific·1985-09-16
• K821687 — REMOVAWELL TISSUE CULTURE PLATE W/LIDDynatech Corp.·1982-06-24
• K790958 — 120 WELL HISTO-PLATEDynatech Laboratories, Inc.·1979-06-28
• K781792 — PRESSURIZER, EXETER CEMENTHowmedica Corp.·1979-02-08